fluticasone propionate diskus
Generic: fluticasone propionate
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
fluticasone propionate diskus
Generic Name
fluticasone propionate
Labeler
a-s medication solutions
Dosage Form
POWDER, METERED
Routes
Active Ingredients
fluticasone propionate 50 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-7076
Product ID
50090-7076_a7be2e79-a4a2-4e3f-a992-a58cd975a829
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA020833
Listing Expiration
2026-12-31
Marketing Start
2023-10-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500907076
Hyphenated Format
50090-7076
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
fluticasone propionate diskus (source: ndc)
Generic Name
fluticasone propionate (source: ndc)
Application Number
NDA020833 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 ug/1
Packaging
- 1 INHALER in 1 CARTON (50090-7076-0) / 60 POWDER, METERED in 1 INHALER
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "a7be2e79-a4a2-4e3f-a992-a58cd975a829", "openfda": {"unii": ["O2GMZ0LF5W"], "rxcui": ["896018"], "spl_set_id": ["64d669da-559c-40f5-b649-2ce164c211ea"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (50090-7076-0) / 60 POWDER, METERED in 1 INHALER", "package_ndc": "50090-7076-0", "marketing_start_date": "20240129"}], "brand_name": "FLUTICASONE PROPIONATE DISKUS", "product_id": "50090-7076_a7be2e79-a4a2-4e3f-a992-a58cd975a829", "dosage_form": "POWDER, METERED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50090-7076", "generic_name": "fluticasone propionate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FLUTICASONE PROPIONATE", "brand_name_suffix": "DISKUS", "active_ingredients": [{"name": "FLUTICASONE PROPIONATE", "strength": "50 ug/1"}], "application_number": "NDA020833", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20231030", "listing_expiration_date": "20261231"}